RNA QC 253 Level 2
Ref QC253-level 2
RNA QC 253 Level 2 (QC 253-2) is an in vitro diagnostic device (EU IVDD general IVD) made by Rna Medical Division, registered in EUDAMED on 27 May 2026 (Basic UDI-DI B-10851290002468) and listed in FDA GUDID since 3 Jun 2019 (UDI-DI 10851290002468), active as of 23 Oct 2026.
Active
CE IVDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDD EUDAMED | NumberB-10851290002468 10851290002468 | Date27 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10851290002468 | Date3 Jun 2019 | StatusListed |
Official records
- EUDAMED public site B-10851290002468
- AccessGUDID record 10851290002468
Across registries
- EUDAMED Basic UDI-DI B-10851290002468 registered 27 May 2026 Active
- FDA GUDID UDI-DI 10851290002468 listed 3 Jun 2019 Listed
Timeline
- Listed FDA GUDID 10851290002468
- Registered EUDAMED B-10851290002468
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- RNA Medical QC 253 Full Range CO-Oximeter Control-level 2 EUDAMEDRNA GUDID
- Generic name
- Total haemoglobin (totHb) IVD, control
- Model / Ref / Catalog
- QC253-level 2 EUDAMEDQC 253 Level 2 GUDIDQC 253-2 GUDID
- Primary DI / UDI-DI
- 10851290002468
- Basic UDI-DI
- B-10851290002468
- EMDN code
- W0101050101 Assayed multicomponent controls (cc)
- GMDN term
- Total haemoglobin (totHb) IVD, control
- Device class
- Class IVD General
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | QC253-level 2 | QC 253 Level 2 |
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